Robust ligand-protein interaction inference reveals off-targets of epigenetic drugs
Ontology highlight
ABSTRACT: Detecting target engagement is a major challenge in drug discovery. To this end, thermal proteome profiling (TPP) offers unbiased assessment of system-wide ligand-protein interactions. However, its most sensitive assay format lacks statistical methods with false discovery rate-control. Here, we present FILIP, a functional data analysis approach and showcase its performance on several TPP-datasets probing epigenetic drugs. This leads us to identify drug off-targets which we validate in vitro.
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): T Cell, Hepatocyte, Monocyte, Cell Culture
SUBMITTER:
Nils Kurzawa
LAB HEAD: Marcus Bantscheff
PROVIDER: PXD016640 | Pride | 2020-10-29
REPOSITORIES: Pride
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